糖尿病视网膜病变的外界膜、光受体椭球区破坏和视网膜色素上皮改变

Nibha Mishra, Gurkiran Kaur, S. Saxena
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引用次数: 0

摘要

摘要目的糖尿病视网膜病变(DR)是糖尿病的微血管并发症,是可预防性失明的主要原因。光谱域光学相干断层扫描(SD-OCT)提供视网膜的横截面和地形成像。SD-OCT将视网膜外层分解为三个高反射带——外限制膜(ELM)、椭球带(EZ)和视网膜色素上皮(RPE)。在本文中,我们研究了这些视网膜外层在DR发生的结构和分子变化中的作用。材料和方法对DR的临床特征、发病机制、诊断和治疗的文章进行了深入的研究。文章在PubMed, MEDLINE和Cochrane图书馆检索,检索时间为2000年至2020年。包括基于SD-OCT的关于ELM、EZ和RPE在DR发病机制中的作用的研究。结果长期高血糖导致蛋白糖基化,形成晚期糖基化终产物(age)。AGEs通过影响视网膜微血管、血管内皮生长因子(VEGF)、细胞间粘附分子-1、亚硝化和氧化应激以及维生素D和钙的代谢来发挥作用。所有这些因素都与视网膜外层的破坏有关。AGEs通过增加视网膜周细胞和RPE细胞中VEGF的表达,导致血管内皮功能障碍和促血管生成因子的释放。这导致渗漏和液体积聚,导致糖尿病性黄斑水肿(DME)。在DME中,ELM和EZ连续中断,视力下降(VA)。据报道,RPE的改变与DR的严重程度和VA的降低有关。抗vegf治疗是DME最常见的治疗方法,可导致ELM屏障作用的恢复,研究发现ELM屏障作用首先恢复,然后是EZ恢复。新的抗ages药物及其受体阻滞剂正在开发中,对维持RPE的健康有积极的作用。结论DR中ELM、EZ和RPE的结构变化存在复杂的分子关联,SD-OCT是研究这些变化不可缺少的工具,因为这些视网膜外层的完整性对于维持DR视网膜的视觉功能至关重要。
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External Limiting Membrane, Photoreceptor Ellipsoid Zone Disruption, and Retinal Pigment Epithelium Alterations in Diabetic Retinopathy
Abstract Objective  Diabetic retinopathy (DR), a microvascular complication of diabetes, is a leading cause of preventable blindness. Spectral domain optical coherence tomography (SD-OCT) provides cross-sectional and topographical imaging of the retina. SD-OCT resolves outer retinal layers into three hyperreflective bands—external limiting membrane (ELM), ellipsoid zone (EZ), and retinal pigment epithelium (RPE). In this article, we have studied the role of these outer retinal layers in structural and molecular changes taking place in DR. Materials and Methods  Articles with clinical features, pathogenesis, diagnosis, and treatment of DR were thoroughly studied. Articles were searched on PubMed, MEDLINE, and Cochrane Library from 2000 to 2020. Studies focusing on the role of ELM, EZ, and RPE in pathogenesis of DR based on SD-OCT were included. Results  The long-standing hyperglycemia leads to protein glycosylation resulting in formation of advanced glycation end products (AGEs). AGEs have an impact through their effect on retinal microvasculature, vascular endothelial growth factor (VEGF), intercellular adhesion molecule-1, nitrosative and oxidative stress, and vitamin D and calcium metabolism. All these factors have been linked with disruption of outer retinal layers. AGEs lead to vascular endothelial dysfunction and release of proangiogenic factors by increasing the expression of VEGF in retinal pericytes and RPE cells. This leads to leakage and fluid accumulation resulting in diabetic macular edema (DME). In DME, there is sequential disruption of ELM and EZ and decrease in visual acuity (VA). The RPE alterations have been reported to be associated with the severity of DR and decrease in VA. Anti-VEGF therapy, most common treatment of DME, leads to restoration of barrier effect of ELM, it was found to be restored first followed by EZ restoration. Newer anti-AGEs agents and their receptor blockers are being developed which have a positive effect on maintaining the health of RPE. Conclusion  A complex molecular association exists between the structural changes in ELM, EZ, and RPE in DR. SD-OCT is an indispensable tool to study these changes as integrity of these outer layers of retina is essential for maintaining visual function of retina in DR.
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